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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 558460Generated: October 25, 2026

Water → 2-(4-Methoxybenzyloxy)-3-bromo-4-methylpyridine

https://huagongshe.com/reaction/558460

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant4-Methoxybenzyl alcoholHCID 7738—
ReactantSodium hydrideHCID 24758—
Reactant3-Bromo-2-chloro-4-methylpyridineHCID 40425119—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
Product2-(4-Methoxybenzyloxy)-3-bromo-4-methylpyridineHCID 67000104—

Reaction Conditions

Temperature75 °C

Reaction Steps

To a mixture of 60% NaH in mineral oil (0.290 g, 7.27 mmol) in THF (15 mL) at RT in a resealable pressure vessel was added (4-methoxyphenyl)methanol (0.906 ml, 7.27 mmol). After 5 minutes, 3-bromo-2-chloro-4-picoline (1.00 g, 4.84 mmol) was added and the mixture was heated to 75° C. After 1 hr, water was added and the mixture was diluted with EtOAc. After washing with water and brine, the organic fraction was dried with sodium sulfate and purified by silica gel chromatography using 0-30% EtOAc:hexanes to afford 2-(4-methoxybenzyloxy)-3-bromo-4-methylpyridine as a colorless oil. M+H+=308.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08063055B2
Source datasetuspto-grants-2011_11
ORD IDord-00729da3fd854147b1d35bcb61d2fdee
Source noteuspto-grants-2011_11